Magnetic properties of six-coordinated high-spin cobalt(II) complexes: Theoretical background and its application |
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Authors: | Francesc Lloret Miguel Julve Joan Cano Rafael Ruiz-García Emilio Pardo |
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Institution: | 1. Departament de Química Inorgànica, Instituto de Ciencia Molecular (ICMol), Universitat de València, Polígono La Coma s/n, 46980 Paterna, València, Spain;2. Departament de Química Inorgànica, Institut de Química Teòrica i Computacional (IQTC), Institut de Nanociència i Nanotecnologia (IN2UB) and Institució Catalana de Recerca I Estudis Avançats (ICREA), Universitat de Barcelona, 08028 Barcelona, Spain |
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Abstract: | In this contribution we study and analyse the influence of the different parameters involved in the magnetic susceptibility of six-coordinated high-spin Co(II) complexes. We propose an empirical expression to fit the magnetic susceptibility of polycrystalline samples of mononuclear Co(II) complexes with an axial distortion, the variable parameters being Δ (axial distortion), α (orbital reduction factor) and λ (spin–orbit coupling). This expression avoids solving the 12 × 12 matrix associated to the distortion of the 4T1g term. In order to take into account the magnetic coupling (J) in the polynuclear Co(II) complexes, a perturbational approach is proposed to describe their magnetic susceptibility in the whole temperature range (2–300 K) as a function of J, Δ, α and λ. This approach is valid in the limit of the weak magnetic coupling as compared to the spin–orbit coupling, |J/λ| < 0.1. The model allows the treatment of each cobalt(II) ion in axial symmetry as an effective spin Seff = 1/2. That causes a drastic reduction of the matrix size of the polynuclear compounds from 12n × 12n to 2n × 2n, n being the number of Co(II) ions in the complex. The main advantage of the model is to make possible the fit of the magnetic susceptibility data of those polynuclear Co(II) complexes whose high nuclearity involved intractable matrices. |
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